Description Usage Arguments Details Value Author(s) References See Also Examples
Function to perform sparse Partial Least Squares (sPLS). The sPLS approach combines both integration and variable selection simultaneously on two data sets in a onestep strategy.
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X 
numeric matrix of predictors. 
Y 
numeric vector or matrix of responses (for multiresponse models).

ncomp 
the number of components to include in the model (see Details).
Default is set to from one to the rank of 
mode 
character string. What type of algorithm to use, (partially) matching
one of 
keepX 
numeric vector of length 
keepY 
numeric vector of length 
scale 
boleean. If scale = TRUE, each block is standardized to zero means and unit variances (default: TRUE) 
tol 
Convergence stopping value. 
max.iter 
integer, the maximum number of iterations. 
near.zero.var 
boolean, see the internal 
logratio 
one of ('none','CLR'). Default to 'none' 
multilevel 
Design matrix for repeated measurement analysis, where multlevel decomposition is required. For a one factor decomposition, the repeated measures on each individual, i.e. the individuals ID is input as the first column. For a 2 level factor decomposition then 2nd AND 3rd columns indicate those factors. See examples. 
all.outputs 
boolean. Computation can be faster when some specific (and nonessential) outputs are not calculated. Default = 
spls
function fit sPLS models with 1, … ,ncomp
components.
Multiresponse models are fully supported. The X
and Y
datasets
can contain missing values.
The type of algorithm to use is specified with the mode
argument. Four PLS
algorithms are available: PLS regression ("regression")
, PLS canonical analysis
("canonical")
, redundancy analysis ("invariant")
and the classical PLS
algorithm ("classic")
(see References and ?pls
for more details).
The estimation of the missing values can be performed
by the reconstitution of the data matrix using the nipals
function. Otherwise, missing
values are handled by casewise deletion in the spls
function without having to
delete the rows with missing data.
logratio transform and multilevel analysis are performed sequentially as internal preprocessing step, through logratio.transfo
and withinVariation
respectively.
Multilevel sPLS enables the integration of data measured on two different data sets on the same individuals. This approach differs from multilevel sPLSDA as the aim is to select subsets of variables from both data sets that are highly positively or negatively correlated across samples. The approach is unsupervised, i.e. no prior knowledge about the sample groups is included.
spls
returns an object of class "spls"
, a list
that contains the following components:
X 
the centered and standardized original predictor matrix. 
Y 
the centered and standardized original response vector or matrix. 
ncomp 
the number of components included in the model. 
mode 
the algorithm used to fit the model. 
keepX 
number of X variables kept in the model on each component. 
keepY 
number of Y variables kept in the model on each component. 
variates 
list containing the variates. 
loadings 
list containing the estimated loadings for the X and Y variates. 
names 
list containing the names to be used for individuals and variables. 
tol 
the tolerance used in the iterative algorithm, used for subsequent S3 methods 
iter 
Number of iterations of the algorthm for each component 
max.iter 
the maximum number of iterations, used for subsequent S3 methods 
nzv 
list containing the zero or nearzero predictors information. 
scale 
whether scaling was applied per predictor. 
logratio 
whether log ratio transformation for relative proportion data was applied, and if so, which type of transformation. 
explained_variance 
amount of variance explained per component (note that contrary to PCA, this amount may not decrease as the aim of the method is not to maximise the variance, but the covariance between data sets). 
input.X 
numeric matrix of predictors in X that was input, before any saling / logratio / multilevel transformation. 
mat.c 
matrix of coefficients from the regression of X / residual matrices X on the Xvariates, to be used internally by 
defl.matrix 
residual matrices X for each dimension. 
Sébastien Déjean, Ignacio González and KimAnh Lê Cao.
Sparse PLS: canonical and regression modes:
Lê Cao, K.A., Martin, P.G.P., RobertGranie, C. and Besse, P. (2009). Sparse canonical methods for biological data integration: application to a crossplatform study. BMC Bioinformatics 10:34.
Lê Cao, K.A., Rossouw, D., RobertGranie, C. and Besse, P. (2008). A sparse PLS for variable selection when integrating Omics data. Statistical Applications in Genetics and Molecular Biology 7, article 35.
Sparse SVD: Shen, H. and Huang, J. Z. (2008). Sparse principal component analysis via regularized low rank matrix approximation. Journal of Multivariate Analysis 99, 10151034.
PLS methods: Tenenhaus, M. (1998). La regression PLS: theorie et pratique. Paris: Editions Technic. Chapters 9 and 11.
Abdi H (2010). Partial least squares regression and projection on latent structure regression (PLS Regression). Wiley Interdisciplinary Reviews: Computational Statistics, 2(1), 97106.
Wold H. (1966). Estimation of principal components and related models by iterative least squares. In: Krishnaiah, P. R. (editors), Multivariate Analysis. Academic Press, N.Y., 391420.
On multilevel analysis:
Liquet, B., Lê Cao, K.A., Hocini, H. and Thiebaut, R. (2012) A novel approach for biomarker selection and the integration of repeated measures experiments from two platforms. BMC Bioinformatics 13:325.
Westerhuis, J. A., van Velzen, E. J., Hoefsloot, H. C., and Smilde, A. K. (2010). Multivariate paired data analysis: multilevel PLSDA versus OPLSDA. Metabolomics, 6(1), 119128.
pls
, summary
,
plotIndiv
, plotVar
,
cim
, network
, predict
, perf
and http://www.mixOmics.org for more details.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72  data(liver.toxicity)
X < liver.toxicity$gene
Y < liver.toxicity$clinic
toxicity.spls < spls(X, Y, ncomp = 2, keepX = c(50, 50),
keepY = c(10, 10))
toxicity.spls < spls(X, Y[,1:2,drop=FALSE], ncomp = 5, keepX = c(50, 50))#, mode="canonical")
## Second example: onefactor multilevel analysis with sPLS, selecting a subset of variables
#
## Not run:
data(liver.toxicity)
# note: we made up those data, pretending they are repeated measurements
repeat.indiv < c(1, 2, 1, 2, 1, 2, 1, 2, 3, 3, 4, 3, 4, 3, 4, 4, 5, 6, 5, 5,
6, 5, 6, 7, 7, 8, 6, 7, 8, 7, 8, 8, 9, 10, 9, 10, 11, 9, 9,
10, 11, 12, 12, 10, 11, 12, 11, 12, 13, 14, 13, 14, 13, 14,
13, 14, 15, 16, 15, 16, 15, 16, 15, 16)
summary(as.factor(repeat.indiv)) # 16 rats, 4 measurements each
# this is a spls (unsupervised analysis) so no need to mention any factor in design
# we only perform a one level variation split
design < data.frame(sample = repeat.indiv)
res.spls.1level < spls(X = liver.toxicity$gene,
Y=liver.toxicity$clinic,
multilevel = design,
ncomp = 3,
keepX = c(50, 50, 50), keepY = c(5, 5, 5),
mode = 'canonical')
# set up colors and pch for plotIndiv
col.stimu < 1:nlevels(design$stimu)
plotIndiv(res.spls.1level, rep.space = 'Xvariate', ind.names = FALSE,
group = liver.toxicity$treatment$Dose.Group,
pch = 20, main = 'Gene expression subspace',
legend = TRUE)
plotIndiv(res.spls.1level, rep.space = 'Yvariate', ind.names = FALSE,
group = liver.toxicity$treatment$Dose.Group,
pch = 20, main = 'Clinical measurements ssubpace',
legend = TRUE)
plotIndiv(res.spls.1level, rep.space = 'XYvariate', ind.names = FALSE,
group = liver.toxicity$treatment$Dose.Group,
pch = 20, main = 'Both Gene expression and Clinical subspaces',
legend = TRUE)
## End(Not run)
## Third example: twofactor multilevel analysis with sPLS, selecting a subset of variables
#
## Not run:
data(liver.toxicity)
dose < as.factor(liver.toxicity$treatment$Dose.Group)
time < as.factor(liver.toxicity$treatment$Time.Group)
# note: we made up those data, pretending they are repeated measurements
repeat.indiv < c(1, 2, 1, 2, 1, 2, 1, 2, 3, 3, 4, 3, 4, 3, 4, 4, 5, 6, 5, 5,
6, 5, 6, 7, 7, 8, 6, 7, 8, 7, 8, 8, 9, 10, 9, 10, 11, 9, 9,
10, 11, 12, 12, 10, 11, 12, 11, 12, 13, 14, 13, 14, 13, 14,
13, 14, 15, 16, 15, 16, 15, 16, 15, 16)
summary(as.factor(repeat.indiv)) # 16 rats, 4 measurements each
design < data.frame(sample = repeat.indiv, dose = dose, time = time)
res.spls.2level = spls(liver.toxicity$gene,
Y = liver.toxicity$clinic,
multilevel = design,
ncomp=2,
keepX = c(10,10), keepY = c(5,5))
## End(Not run)

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